城市人为热排放分类研究及其对气温的影响

随着城市化进程日益加速，城市热岛现象愈发严重。利用上海市近50 a各区县月均温数据，统计分析了各区与崇明夏季每5 a均温差，发现热岛效应由市区中心向郊区延伸，范围越来越大，特别是20世纪80年代开始温差呈较大幅增加，城市热岛现象显著；在前人工作的基础上，分析热岛产生机制中的主要原因之一：城市中人为热排。绘制人为热排放流程图，并将城市人为热源进行分类，分析所有可能成为人为热排放源的设施以便定性及控制研究；对供给，消费和排出3种阶段的计算方法进行对比归纳，根据目的不同分别使用；分别计算燃油排热和燃煤排热以估算上海市人为热排放总量，统计上海市区和郊区的年均温及年均温差随时间变化及其与人为热排放之间的关系，发现两者之间有很好的相关性；最后就上海市夏季空调使用排热对上海市温度影响进行了定性研究，数字化上海市航片得到上海市建筑物分布图，假设楼层和空调密度之间存在相关性，发现空调排热与地面温度反演有着非常良好的一致性，同时也是造成上海城市高温的主要因素之一     

Heavy Metal Distribution in Valley Sediments in Wadi Al-Karak Catchment Area, South Jordan

Valley sediments samples collected from the major and minor valleys of Al-Karak catchment area (southern Jordan) were leached with hot dilute HCl and analysed for their heavy metals content. The results of leachable metal concentrations indicated the absence of anomalous values for metal occurrences. However, appreciable contamination of the sediments with Cu, Zn, Pb, Cd and Cr was observed. Using an index of pollution the extent of contamination was better delineated. The geographical distribution of the samples showed higher Cu, Zn, Pb, Cd and Cr concentrations mainly around heavily inhabited areas indicating an anthropogenic source of contamination. Lithological influence indicated from the anomalies of Fe and Mn was found to be very low.     

利用SPAMS研究南宁市冬季单颗粒气溶胶化学成分

利用单颗粒气溶胶飞行时间质谱仪(SPAMS)对南宁市2015年冬季2月15~24日期间大气PM2.5进行观测.SPAMS所测得大气PM2.5数浓度与PM2.5质量浓度线性相关系数为0.76,在一定程度上颗粒物数浓度可反映大气污染状况.利用自适应共振神经网络分类方法(Art-2a)对PM2.5化学成分进行分类,确定PM2.5化学成分主要为元素碳、有机元素碳混合颗粒、有机碳、富钾颗粒、矿物质、富钠颗粒、二次无机颗粒、左旋葡聚糖以及其它重金属共9类.成分占比最高的是元素碳,其次是有机碳和富钾颗粒.监测到80%以上的PM2.5粒径主要集中在0.2~1.0μm之间,峰值出现在0.62μm处,各化学成分的粒径分布特征与总颗粒数粒径分布特征相似.各化学成分数浓度与PM2.5质量浓度随时间变化趋势较一致,化学成分数浓度占比变化在一定程度上可反映瞬时的污染来源.     

Role of secondary aerosols in haze formation in summer in the Megacity Beijing

A field experiment from 18 August to 8 September 2006 in Beijing, China, was carried out. A hazy day was defined as visibility 10 km and RH(relative humidity) 90%. Four haze episodes, which accounted for ~ 60% of the time during the whole campaign, were characterized by increases of SNA(sulfate, nitrate, and ammonium) and SOA(secondary organic aerosol) concentrations. The average values with standard deviation of SO2-+4, NO-3, NH4 and SOA were 49.8(± 31.6), 31.4(±22.3), 25.8(±16.6) and 8.9(±4.1) μg/m3, respectively, during the haze episodes, which were 4.3, 3.4, 4.1, and 1.7 times those in the non-haze days. The SO2-4,NO-3, NH+4, and SOA accounted for 15.8%, 8.8%, 7.3%, and 6.0% of the total mass concentration of PM10 during the non-haze days. The respective contributions of SNA species to PM10 rose to about27.2%, 15.9%, and 13.9% during the haze days, while the contributions of SOA maintained the same level with a slight decrease to about 4.9%. The observed mass concentrations of SNA and SOA increased with the increase of PM10 mass concentration, however, the rate of increase of SNA was much faster than that of the SOA. The SOR(sulfur oxidation ratio) and NOR(nitrogen oxidation ratio) increased from non-haze days to hazy days, and increased with the increase of RH. High concentrations of aerosols and water vapor favored the conversion of SO2 to SO2-4and NO2 to NO-3, which accelerated the accumulation of the aerosols and resulted in the formation of haze in Beijing.     

长江三角洲城市群人为热排放特征研究

基于常规可获取的能源、交通、人口等统计资料,利用“自上而下”的能源清单法,研究了2010年长江三角洲(以下简称“长三角”)城市群地区各类人为热排放量及其时空分布特征.结果表明:该地区人为热排放总量为1.4′1019J/a,其中工业、交通、建筑、新陈代谢分别占75.1%、12.5%、9.9%和2.5%.上海、苏州、无锡、杭州和南京五个城市的人为热排放总量约占研究区域总量的71%.长三角城市群的人为热年平均排放通量为5.3W/m2,大部分地区介于5~30W/m2,城市高值区一般介于20~70W/m2,上海明显高于其他城市.为方便有关环境气候模式的输入,本文提供了人为热排放的网格化空间分布和简单的时间变化廓线.     

On the horizontal homogeneity of mass-related aerosol properties

We studied the mass-related aerosol properties, simultaneously attwo sites at the urban roof top level in the same city. Nosystematic influence of the wind vector on the difference in theaerosol concentrations between the two locations could be found.These results are compared with results from a second, similarexperiment over a larger distance including one urban and onerural site. Surprisingly, we could not detect a tendency whichwould indicate that sampling air at distance in the order of 1 kmwould be less affected by the heterogeneity than samplingdistanced in the order of 10 km apart. On the contrary, theresults suggest that mass-related properties at two sites in thesame city are not necessarily more similar than at an urban and arural site outside the city. These results stress the limitedhorizontal homogeneity of urban atmospheric aerosol. As aconclusion it is suggested that single-site measurements of mass-related aerosol properties should be considered to berepresentative for an area smaller than 1 km² on size.     

Deposition of Inorganic Particulate Aerosols to Vegetation - A New Method of Estimating

A new, direct method was developed for quantifying inorganic particulate aerosols trapped by the forest canopy, and for determining the resulting input of elements to a forest ecosystem. The method is based on direct measurements of only six parameters. Using this method, it is possible to determine the load of aerosols trapped by the forest canopy and deposited to leaves, as well as the load of aerosols falling to the forest floor by impaction on plants. It is also possible to estimate the aerosol input of soluble and insoluble elements to an ecosystem. With this new method it has been found that the load of aerosols trapped by the canopy of a mixed forest located in the Rybnik Coal Basin averaged 189.0 kg x ha-1 x growing season-1, or 39.3% of the total inorganic particles reaching the ecosystem. The trapped aerosols provided 13.4 kg x ha-1 of soluble nitrogen and 0.91 kg x ha-1 of insoluble nitrogen over the growing season. At the same time, the input of soluble nitrogen from the atmosphere with rainfall to an open area averaged 13.9 kg x ha-1, and the input of insoluble nitrogen with inorganic dusts averaged 1.4 kg x ha-1.     

A Three-Dimensional Model Study of the Impact of AVOC and BVOC Emissions on Ozone in an Urban Area of the Eastern Spain

This study concentrated on the effects of Biogenic Volatile Organic Compounds (BVOC) emissions on ozone (O₃) in an area of the Eastern Spain on June 12, 1997, a day characterised by sea breeze. Simulation of meteorology was performed with the three-dimensional model ADREA-I. Comparisons of the model results with observations have revealed overall a good agreement in temperature and wind velocity. Two runs were performed with UAM-IV for the photochemical calculations. The first simulated the effects of the anthropogenic emissions only (run A) and the second the combined effects of anthropogenic and biogenic emissions, (run B). Comparisons of the model O₃ concentrations with measurements showed a general agreement with the experimental data. Discrepancies between the calculated results and the observations during the early morning hours could be attributed to inaccuracies in nitrogen oxides (NO_x) from the anthropogenic emissions inventory. Comparisons between runs A and B yielded differences up to 30% in the morning, over inland areas. It was deduced that the inclusion of BVOC in total emissions could result in an increase or decrease of tropospheric O₃, depending on the available amounts of anthropogenic emissions.     

Anthropogenic Calcium Particles Observed in Beijing and Qingdao, China

Analysis of individual particles collected at Beijing in northern China revealed that particles abundant in calcium (Ca) always constituted a large fraction of mineral particles in the urban atmosphere. The particles were characterized by cubic morphologies. The major mineral element in the particles was Ca and few or no other mineral elements were detected. A large number of the particles were in the range of diameter <1 μm, where common natural mineral particles were rarely detected. The contribution of the Ca particles to the volume of total mineral particles greatly exceeded that of other mineral particles during non-dust-storm periods and was comparable to that during dust-storm periods. Reagent film tests showed that particulate sulfate and nitrate formation on the Ca particles was similar to that on common mineral particles. These results indicate that a large portion of Ca in the atmospheric particulate matter in Beijing was from anthropogenic sources rather than from natural sources, and the anthropogenic Ca particles acted as a significant medium for the formation of sulfate and nitrate. Similar particles were also detected at Qingdao, a coastal city in northern China. Data of a dust storm event showed that Ca-abundant particles from East China arrived there and moved out of the continent, similarly to Asian dust storm particles, suggesting possible contributions of anthropogenic Ca even in Asian dust storm samples in the downstream areas. Therefore, Ca may not be a good indicator of Asian dust from natural sources. However, the Ca particles, due to their unique shapes and elemental compositions, may provide an indicator for the atmospheric dispersion of anthropogenic particulate matters in East Asia.     

Characteristics of Cajander Larch (<Emphasis Type="Italic">Larix cajanderi</Emphasis> Mayr) on Dredging Waste Dumps in the Amur Region

Former dredging sites were studied in the taiga zone of the Amur region (in Khabarovsk Krai). The involvement of Larix cajanderi in plant succession on dredging waste dumps was revealed. Some morphological-anatomical parameters of L. cajanderi needles were compared in trees growing on the dumps and in adjacent open larch stands on waterlogged peaty soils.__________Translated from Ekologiya, No. 4, 2005, pp. 259–263.Original Russian Text Copyright © 2005 by Osipov, Burundukova.